Ethyl 3-methyl-5-amino-1-(2,3-O-isopropylidene-a- and -β-D- ribofuranosyl)imidazolium-4-carboxylate iodides, the corresponding benzyl-β-D-ribofuranosyl ester, and benzyl 3-methyl-5-amino-1-(2,3,5-tri-O- acetyl-β-D-ribofuranosyl)imidazolium-4-carboxylate iodide have been prepared by methylation of the corresponding nucleosides with methyl iodide. Their reactions with acids and bases have been examined. Ethyl 4(5)-methylamino- and dimethylamino-imidazole-5(4)-carboxylates have been prepared in a sequence of reactions from ethyl cyanoacetate and the former compound was converted into 3-methylhypoxanthine by heating with formamidine acetate and into 3-methylguanine by a sequence of reactions. The methylamino-derivative undergoes a Dimroth rearrangement when heated with aqueous ammonia, to produce 1-methyl-5-aminoimidazole-carboxamide.

Type

Journal article

Journal

Journal of the Chemical Society, Perkin Transactions 1

Publication Date

01/12/1979

Pages

3107 - 3112